| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs6295 | 0.645 | 0.200 | 5 | 63962738 | intron variant | C/G | snv | 0.49 | 40 | ||
| rs1800044 | 0.827 | 0.200 | 5 | 63961061 | missense variant | C/A | snv | 3.7E-03 | 3.8E-03 | 8 | |
| rs878567 | 0.882 | 0.040 | 5 | 63960164 | intron variant | A/C;G | snv | 4 | |||
| rs1800041 | 0.882 | 0.120 | 5 | 63961673 | missense variant | G/A | snv | 1.8E-03 | 5.3E-04 | 4 | |
| rs1799920 | 5 | 63961656 | missense variant | C/G;T | snv | 3.2E-04 | 2 | ||||
| rs1799921 | 5 | 63961638 | missense variant | T/C | snv | 9.4E-03 | 9.3E-03 | 2 | |||
| rs1800042 | 1.000 | 0.040 | 5 | 63960902 | missense variant | C/A;T | snv | 8.0E-06; 1.4E-03 | 2 | ||
| rs113195492 | 1.000 | 0.040 | 5 | 63962787 | intron variant | C/T | snv | 8.8E-04 | 1 |